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Zileuton-d4 (major)
Zileuton-d4 (major)
United States Biological

An inhibitor of 5-lipoxygenase, the initial enzyme in the biosynthesis of leukotrienes from Arachidonic Acid. Used as an antiasthmatic. Form: White Solid...

CP-10447
CP-10447
United States Biological

An inhibitor apolipoprotein B (apoB) and triglyceride secretion in human hepatoma cells (HepG2) by inhibiting MTP activity and stimulating the early ER...

1-Acetyl-2,3-dihydro-2-methyl-1H-indol-5-ol
1-Acetyl-2,3-dihydro-2-methyl-1H-indol-5-ol
United States Biological

An indole derivative. Form: Pale Brown Solid Solubility: Dichlormethane, Dimethyl Formamide, Ethyl Acetate, Methanol

Indoline
Indoline
United States Biological

An indole derivative used in the preparation of various medicinal compounds such as potential a1-adrenoceptor (a1-AR) antagonists. Form: Pale Yellow Oil...

5-Methoxy-2-methylindole
5-Methoxy-2-methylindole
United States Biological

An indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic...

7-(Trifluoromethyl)1H-indole-2,3-dione
7-(Trifluoromethyl)1H-indole-2,3-dione
United States Biological

An indole derivative as inhibitor of COX-1, COX-2, and b-catenin. Useful in the treatment of diseases such as: lung cancer, diabetes and Alzheimer's disease....

Reserpine
Reserpine
United States Biological

An indole alkaloid found in Rauwolfia serpentina. Inhibits vesicular uptake of catecholamines and serotonin. Reserpine is reasonably anticipated to be a...

Thromboxane B2
Thromboxane B2
United States Biological

An inactive metabolite/product of Thromboxane A2 (TBXA2): a compound involved in platelet activation and aggregation in case of a wound. Urinary analysis of...

Isochlortetracycline
Isochlortetracycline
United States Biological

An inactive metabolite of Chlortetracycline (CTC). Form: Beige Solid Melting Point: 202-205 degrees C (dec.) Solubility: Aqueous Base, DMSO

cis-Nabilone
cis-Nabilone
United States Biological

An inactive isomer of Nabilone Form: White Solid Solubility: Acetone, Dichloromethane, Methanol

cis-Nabilone
cis-Nabilone
United States Biological

An inactive isomer of Nabilone Form: White Powder Solid Solubility: Acetone, Dichloromethane, Methanol

Pidotimod Diketopiperazine
Pidotimod Diketopiperazine
United States Biological

An impurity product of Pidotimod. Form: White to Off-White Solid Melting Point: 208-210 degrees C Solubility: Chloroform

Pidotimod Diketopiperazine-6-propanoic Acid
Pidotimod Diketopiperazine-6-propanoic Acid
United States Biological

An impurity product of Pidotimod. Form: Off-White Solid Melting Point: 50-52 degrees C Solubility: DMSO, Methanol

Homoveratronitrile
Homoveratronitrile
United States Biological

An impurity of Verapamil. An intermediate in the preparation of the muscle relaxant Papverine. Form: White Solid Melting Point: 64-66 degrees C Solubility:...

4-Desmethoxy-4-bromo Trimethoprim
4-Desmethoxy-4-bromo Trimethoprim
United States Biological

An impurity of Trimethoprim with inhibitory effects on the enzyme dihydrofolate reductase.

4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide  (Torsemide impurity)
4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide (Torsemide impurity)
United States Biological

An impurity of Torsemide. Form: Tan Solid Melting Point: 168-170 degrees C Solubility: DMSO, Methanol

Deoxystreptamine-kanosaminide
Deoxystreptamine-kanosaminide
United States Biological

An impurity of Tobramycin. Form: Off-White Solid Melting Point: >135 degrees C (dec.) Solubility: Water

5-Hydroxy-2-[1-methyl-1-[[benzylcarbamoyl]amino]ethyl]-6-methoxypyrimidine-4-carboxylic Acid Methyl Ester
5-Hydroxy-2-[1-methyl-1-[[benzylcarbamoyl]amino]ethyl]-6-methoxypyrimidine-4-carboxylic Acid Methyl Ester
United States Biological

An impurity of the commercial synthesis of Raltegravir Form: Off-White Solid Melting Point: 108-112 degrees C Solubility: DMSO, Methanol

Desfluoro Ezetimibe
Desfluoro Ezetimibe
United States Biological

An impurity of the cholesterol absorption inhibitor Ezetimibe.

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